The Turner Syndrome Foundation’s (TSF) My Story blog series highlights the experiences of individuals, families, and caregivers impacted by Turner Syndrome (TS). Their stories have an incredible ability to inspire others and make a positive impact on the TS community….
Read MoreThe Turner Syndrome Foundation’s (TSF) My Story blog series highlights the experiences of individuals, families, and caregivers affected by Turner Syndrome (TS). Their stories have an incredible ability to inspire others and make a positive impact on the TS community….
Read MoreTurner Syndrome (TS) is a genetic condition that affects 1 in every 2,000 live female births. Individuals with TS usually have short stature, may be infertile, and may experience a variety of medical, cognitive, and psychological challenges. Given these challenges,…
Read MoreThe importance of early cardiac evaluation and intervention for those with Turner Syndrome (TS) cannot be stressed enough. In this post, we will explore a study that highlights the different cardiovascular risks for TS patients and their connection to endocrine…
Read MoreOngoing, specialized medical care is essential for those with Turner Syndrome (TS). The Turner Syndrome Foundation (TSF) offers a Professional Membership Program for healthcare professionals to network, share resources, and register themselves as TS providers in our registry. Communication is…
Read MoreOne of the main goals of the Turner Syndrome Foundation (TSF) is to educate medical professionals and institutions on important research that can help patients with Turner Syndrome (TS). In this post, we summarize the research paper “Social Skills and…
Read MoreNew Resource for Expectant Parents: Prenatal Testing & Information About Turner Syndrome booklet. Learn more
Read MoreRaising Daughters Now and Then Today is Daughter’s Day 2021, a day in society where being a daughter and having a daughter means something completely different than it did even a few years ago. Women are teaching their young daughters…
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